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RECRUITINGPhase 2INTERVENTIONAL

Azithromycin Treatment of Hospitalized Children With Asthmatic Symptoms

Azithromycin Treatment of Hospitalized Children With Asthmatic Symptoms: A Double-blinded, Randomized, Controlled Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of this double-blind, randomized, controlled clinical trial is to investigate the effect of a three-day azithromycin treatment versus placebo treatment in children aged 1-5 years who are hospitalized due to asthma-like symptoms.

Who May Be Eligible (Plain English)

Who May Qualify: - Previous episode(s) with asthma-like symptoms and / medical treatment with SABA as mono-therapy or SABA in combination with ICS and possibly LTRA. - The parent/guardian(s) agrees to admit the child and is willing to follow the procedure of the trial. - The child is between 12-71 months old. - Fluent Danish skills with parents / guardians. Who Should NOT Join This Trial: - Known allergy to macrolide antibiotics. - Known impaired liver function. - Known renal impairment. - Known with neurological or psychiatric diseases. - Known with congenital or documented acquired QT interval. - Known for clinically relevant bradycardia, cardiac arrhythmia or severe heart failure. - Clinical signs of pneumonia (Objective findings, including severe tachypnoea: respiratory rate (RF)\> 50 and / or Fever: temperature\> 39 °C and / or C-reactive protein (CRP)\> 50). Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Previous episode(s) with asthma-like symptoms and / medical treatment with SABA as mono-therapy or SABA in combination with ICS and possibly LTRA. * The parent/guardian(s) agrees to admit the child and is willing to follow the procedure of the trial. * The child is between 12-71 months old. * Fluent Danish skills with parents / guardians. Exclusion Criteria: * Known allergy to macrolide antibiotics. * Known impaired liver function. * Known renal impairment. * Known with neurological or psychiatric diseases. * Known with congenital or documented acquired QT interval. * Known for clinically relevant bradycardia, cardiac arrhythmia or severe heart failure. * Clinical signs of pneumonia (Objective findings, including severe tachypnoea: respiratory rate (RF)\> 50 and / or Fever: temperature\> 39 °C and / or C-reactive protein (CRP)\> 50).

Treatments Being Tested

DRUG

Azithromycin Oral Liquid Product

10 mg/kg for 3 consecutive days

OTHER

Placebo mixture

Placebo mixture containing no active substance

Locations (1)

University Hospital of Copenhagen
Gentofte Municipality, Denmark